Variant report

Variant	nsv1015477
Chromosome Location	chr5:178954409-179016804
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1610)
CpG islands
(count:2810)
Chromatin interactive
region (count:112)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1610 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178985842-178986538	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178977115-178977357	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:178977590-178977818	HepG2	liver:	n/a	n/a
4	ATF2	chr5:178985934-178986763	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:178960873-178961287	GM12878	blood:	n/a	n/a
6	ATF2	chr5:178976968-178977468	GM12878	blood:	n/a	n/a
7	ATF2	chr5:178977014-178977777	GM12878	blood:	n/a	n/a
8	ATF2	chr5:178971353-178972009	GM12878	blood:	n/a	n/a
9	ATF2	chr5:178986020-178986776	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr5:178971356-178971893	GM12878	blood:	n/a	n/a
11	BACH1	chr5:178976363-178976432	K562	blood:	n/a	n/a
12	BACH1	chr5:178957142-178957774	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr5:178977696-178978347	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr5:178971440-178971812	GM12878	blood:	n/a	chr5:178971650-178971659
15	BCL11A	chr5:178971422-178971880	GM12878	blood:	n/a	chr5:178971650-178971659
16	BCL3	chr5:178995617-178995986	GM12878	blood:	n/a	n/a
17	BCL3	chr5:178999749-179000029	GM12878	blood:	n/a	n/a
18	BCL3	chr5:178986050-178987128	A549	lung:	n/a	n/a
19	BCL3	chr5:178995361-178995595	GM12878	blood:	n/a	n/a
20	BCL3	chr5:178985836-178986998	A549	lung:	n/a	n/a
21	BCLAF1	chr5:178971380-178972055	GM12878	blood:	n/a	chr5:178971650-178971659
22	BCLAF1	chr5:178977094-178977496	GM12878	blood:	n/a	chr5:178977430-178977439
23	BCLAF1	chr5:178977522-178978403	GM12878	blood:	n/a	chr5:178978060-178978073 chr5:178978272-178978285 chr5:178978064-178978077
24	BHLHE40	chr5:178977555-178978270	HepG2	liver:	n/a	chr5:178978066-178978082 chr5:178978012-178978028
25	BHLHE40	chr5:179012837-179013284	K562	blood:	n/a	n/a
26	BHLHE40	chr5:178976912-178978367	GM12878	blood:	n/a	chr5:178978066-178978082 chr5:178978012-178978028 chr5:178978259-178978275
27	BHLHE40	chr5:178977025-178978380	K562	blood:	n/a	chr5:178978066-178978082 chr5:178978012-178978028 chr5:178978259-178978275
28	BHLHE40	chr5:178967579-178967940	HepG2	liver:	n/a	n/a
29	BHLHE40	chr5:178971425-178971980	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:178960996-178961233	GM12878	blood:	n/a	n/a
31	BRCA1	chr5:178985953-178986744	H1-hESC	embryonic stem cell:	n/a	n/a
32	CBX3	chr5:178985780-178986131	K562	blood:	n/a	n/a
33	CBX3	chr5:178957621-178958014	K562	blood:	n/a	n/a
34	CCNT2	chr5:178957677-178957915	K562	blood:	n/a	n/a
35	CCNT2	chr5:178977542-178978403	K562	blood:	n/a	n/a
36	CEBPB	chr5:179010306-179010330	HepG2	liver:	n/a	n/a
37	CEBPB	chr5:178975626-178976364	HepG2	liver:	n/a	chr5:178975778-178975789
38	CEBPB	chr5:178980904-178981262	IMR90	lung:	n/a	n/a
39	CEBPB	chr5:178973974-178974068	H1-hESC	embryonic stem cell:	n/a	chr5:178974017-178974028
40	CEBPB	chr5:178977272-178977473	K562	blood:	n/a	n/a
41	CEBPB	chr5:178977303-178977503	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:178969684-178970146	Hela-S3	cervix:	n/a	chr5:178969816-178969827
43	CEBPB	chr5:178975674-178975843	HepG2	liver:	n/a	chr5:178975778-178975789
44	CEBPB	chr5:178985853-178986832	A549	lung:	n/a	n/a
45	CEBPB	chr5:178975670-178975842	H1-hESC	embryonic stem cell:	n/a	chr5:178975778-178975789
46	CEBPB	chr5:178961512-178961808	HepG2	liver:	n/a	n/a
47	CEBPB	chr5:178969712-178969909	HepG2	liver:	n/a	chr5:178969816-178969827
48	CEBPB	chr5:178969707-178969953	K562	blood:	n/a	chr5:178969816-178969827
49	CEBPB	chr5:178980961-178981234	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr5:179016185-179016305	HepG2	liver:	n/a	n/a

(count:2810 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178986404-178986454	Hepatocyte	liver:	n/a
2	chr5:178957880-178957930	HL-60	blood:	n/a
3	chr5:178957880-178957930	SK-N-SH_RA	brain:	n/a
4	chr5:179004739-179004789	HRE	kidney:	n/a
5	chr5:178986404-178986454	Hepatocyte	liver:	n/a
6	chr5:178957880-178957930	HL-60	blood:	n/a
7	chr5:178957880-178957930	SK-N-SH_RA	brain:	n/a
8	chr5:179004739-179004789	HRE	kidney:	n/a
9	chr5:178978460-178978510	AG09319	gingival:	n/a
10	chr5:178978460-178978510	T-47D	breast:	n/a
11	chr5:178977123-178977173	H1-hESC	embryonic stem cell:	embryo
12	chr5:178960377-178960427	T-47D	breast:	n/a
13	chr5:178957434-178957484	HUVEC	blood vessel:	n/a
14	chr5:179004535-179004585	HEK293	kidney:	embryo
15	chr5:178977375-178977425	IMR90	lung:	fetal
16	chr5:178957344-178957394	GM12878	blood:	n/a
17	chr5:178986728-178986778	HNPCEpiC	eye:	n/a
18	chr5:178986412-178986462	NHBE	bronchial:	n/a
19	chr5:179003843-179003893	HAEpiC	amniotic membrane:	n/a
20	chr5:178956874-178956924	NT2-D1	testis:	n/a
21	chr5:178986830-178986880	CMK	blood:	n/a
22	chr5:178960377-178960427	AG09309	skin:	n/a
23	chr5:178977377-178977427	CMK	blood:	n/a
24	chr5:179004707-179004757	HCF	heart:	n/a
25	chr5:178956874-178956924	HRE	kidney:	n/a
26	chr5:178986830-178986880	BE2_C	brain:	n/a
27	chr5:178982556-178982606	CMK	blood:	n/a
28	chr5:178973820-178973870	HRCEpiC	kidney:	n/a
29	chr5:179004757-179004807	K562	blood:	n/a
30	chr5:179003843-179003893	PrEC	prostate:	n/a
31	chr5:178977641-178977691	BE2_C	brain:	n/a
32	chr5:178987429-178987479	HIPEpiC	eye:	n/a
33	chr5:178978234-178978284	GM12891	blood:	n/a
34	chr5:178977521-178977571	HEK293	kidney:	embryo
35	chr5:178957930-178957980	PrEC	prostate:	n/a
36	chr5:179003843-179003893	U87	brain:	n/a
37	chr5:178977406-178977456	Hepatocyte	liver:	n/a
38	chr5:178986906-178986956	Jurkat	blood:	n/a
39	chr5:178977648-178977698	Hela-S3	cervix:	n/a
40	chr5:178957598-178957648	HIPEpiC	eye:	n/a
41	chr5:178957598-178957648	AG10803	skin:	n/a
42	chr5:178957344-178957394	T-47D	breast:	n/a
43	chr5:178990055-178990105	Jurkat	blood:	n/a
44	chr5:178978460-178978510	HUVEC	blood vessel:	n/a
45	chr5:178980927-178980977	HepG2	liver:	n/a
46	chr5:179004757-179004807	HEK293	kidney:	embryo
47	chr5:178957598-178957648	Caco-2	colon:	n/a
48	chr5:178977521-178977571	ProgFib	skin:	n/a
49	chr5:178986728-178986778	NT2-D1	testis:	n/a
50	chr5:179006403-179006453	T-47D	breast:	n/a

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:178967564..178969306-chr5:178978047..178979581,2	K562	blood:
2	chr5:178976253..178979060-chr5:179002246..179003961,2	K562	blood:
3	chr5:178977295..178978049-chrX:153718720..153719639,2	Hela-S3	cervix:
4	chr5:178976539..178978410-chr5:179046983..179049342,2	MCF-7	breast:
5	chr5:178955819..178957353-chr5:179123603..179125281,2	MCF-7	breast:
6	chr5:178986818..178988892-chr5:179105129..179106638,2	K562	blood:
7	chr5:178953283..178956112-chr5:178976067..178979094,3	MCF-7	breast:
8	chr5:178961944..178964885-chr5:178975318..178977306,2	MCF-7	breast:
9	chr5:179011616..179013589-chr5:179034982..179036835,2	K562	blood:
10	chr5:178986726..178988892-chr5:179104044..179106638,2	K562	blood:
11	chr5:178976288..178979908-chr5:179158372..179161228,3	MCF-7	breast:
12	chr5:178975801..178977799-chr5:178987617..178990258,3	K562	blood:
13	chr5:178958501..178962397-chr5:178966368..178969379,3	K562	blood:
14	chr5:178966233..178969209-chr5:178970782..178972509,2	MCF-7	breast:
15	chr1:110881782..110882370-chr5:178977392..178978012,2	Hela-S3	cervix:
16	chr5:178959529..178962397-chr5:178966368..178968696,2	K562	blood:
17	chr5:178979685..178981490-chr5:178983248..178984975,2	K562	blood:
18	chr5:178951884..178954426-chr5:179031332..179033126,2	MCF-7	breast:
19	chr5:178980836..178983768-chr5:179095589..179098241,2	MCF-7	breast:
20	chr5:178989647..178992005-chr5:179000001..179001767,2	K562	blood:
21	chr5:178960272..178962115-chr5:178969166..178970829,2	MCF-7	breast:
22	chr5:179001067..179003316-chr5:179026144..179027789,2	MCF-7	breast:
23	chr5:178958501..178962397-chr5:178966368..178969379,3	K562	blood:
24	chr5:179011326..179015421-chr5:179015501..179018945,4	MCF-7	breast:
25	chr5:178976299..178979036-chr5:178987617..178989903,2	K562	blood:
26	chr5:178947804..178950473-chr5:178974779..178977233,2	MCF-7	breast:
27	chr5:179004969..179007855-chr5:179049122..179050815,2	MCF-7	breast:
28	chr5:177630883..177632521-chr5:178985029..178986804,2	MCF-7	breast:
29	chr5:178976591..178978128-chr5:179049452..179051597,2	MCF-7	breast:
30	chr5:178993088..178996882-chr5:179048174..179052059,4	K562	blood:
31	chr5:178967863..178970636-chr5:179244489..179247315,2	MCF-7	breast:
32	chr5:178996663..178999644-chr5:179000508..179002723,3	K562	blood:
33	chr5:178990186..178992537-chr5:178996461..178998253,2	K562	blood:
34	chr5:178964680..178966401-chr5:178977965..178979894,2	K562	blood:
35	chr5:178966233..178969209-chr5:178970782..178972509,2	MCF-7	breast:
36	chr5:178984205..178987569-chr5:178988108..178992792,6	MCF-7	breast:
37	chr15:101835145..101835812-chr5:178986003..178986591,2	HCT-116	colon:
38	chr5:178958463..178961720-chr5:178975691..178978032,4	MCF-7	breast:
39	chr5:178975871..178983601-chr5:179047224..179052413,15	K562	blood:
40	chr5:178984878..178986642-chr5:178988155..178989998,2	MCF-7	breast:
41	chr5:178975751..178978306-chr5:178993914..178996502,2	MCF-7	breast:
42	chr5:178966269..178968602-chr5:178984458..178986550,2	MCF-7	breast:
43	chr5:178967183..178969964-chr5:178976742..178979184,3	MCF-7	breast:
44	chr5:178990186..178992537-chr5:178996461..178998253,2	K562	blood:
45	chr5:178979685..178981544-chr5:178981841..178984975,3	K562	blood:
46	chr5:178985192..178988541-chr5:179048594..179052191,5	MCF-7	breast:
47	chr5:178975690..178977861-chr5:179029775..179032308,2	K562	blood:
48	chr5:178976329..178981059-chr5:179123787..179127407,6	K562	blood:
49	chr5:179008184..179011132-chr5:179049089..179051840,4	MCF-7	breast:
50	chr5:178971437..178973246-chr5:178974311..178976700,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPH1-4	chr5:178975273-178975507	expReg_chr5_10798_-
2	lnc-RUFY1-3	chr5:178971224-178972983	NONHSAT105589
3	lnc-AC136604.1-5	chr5:178999157-178999742	NONHSAT105590

No data

Variant related genes	Relation type
PRDX2P3	TF binding region
ENSG00000253520	TF binding region
RUFY1	TF binding region
PRDX2P3	CpG island
ENSG00000253520	CpG island
RUFY1	CpG island
ENSG00000176783	chromatin interactions
ENSG00000259172	chromatin interactions
ENSG00000167716	chromatin interactions
ENSG00000227963	chromatin interactions
ENSG00000139644	chromatin interactions
ENSG00000161021	chromatin interactions
ENSG00000131876	chromatin interactions
ENSG00000248275	chromatin interactions
ENSG00000249140	chromatin interactions
ENSG00000251545	chromatin interactions
ENSG00000127022	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000161011	chromatin interactions
ENSG00000244945	chromatin interactions
ENSG00000225051	chromatin interactions
ENSG00000153575	chromatin interactions
ENSG00000126903	chromatin interactions
ENSG00000183718	chromatin interactions
ENSG00000221394	chromatin interactions
ENSG00000253520	chromatin interactions
ENSG00000186594	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000162775	chromatin interactions

Extended variants
information (count: 2573 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2573 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373050722	chr5:178954477-178954478	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs566374263	chr5:178954485-178954486	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs367597373	chr5:178954543-178954544	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs528781817	chr5:178954560-178954561	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs547335678	chr5:178954561-178954562	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs56896921	chr5:178954600-178954601	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs539240065	chr5:178954624-178954625	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs557133040	chr5:178954632-178954633	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs569323109	chr5:178954633-178954634	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs372864775	chr5:178954637-178954638	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs74842239	chr5:178954737-178954738	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554925346	chr5:178954743-178954744	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs183514708	chr5:178954744-178954745	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540101617	chr5:178954809-178954810	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs558447146	chr5:178954836-178954837	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs187853175	chr5:178954866-178954867	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs57031671	chr5:178954912-178954913	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs114627732	chr5:178954914-178954915	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs76173386	chr5:178954915-178954916	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs541595526	chr5:178954918-178954919	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs560061778	chr5:178954996-178954997	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs527308198	chr5:178955026-178955027	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs10035797	chr5:178955046-178955047	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs561907208	chr5:178955086-178955087	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs568666607	chr5:178955105-178955106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs534421279	chr5:178955110-178955111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs371933458	chr5:178955114-178955115	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs116738400	chr5:178955301-178955302	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs551148923	chr5:178955326-178955327	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs568597703	chr5:178955331-178955332	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536733657	chr5:178955337-178955338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192310584	chr5:178955344-178955345	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs113864913	chr5:178955354-178955355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs533933832	chr5:178955404-178955405	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs558570264	chr5:178955411-178955412	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs190403918	chr5:178955424-178955425	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs537779367	chr5:178955425-178955426	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs556308756	chr5:178955444-178955445	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574563977	chr5:178955445-178955446	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181717458	chr5:178955467-178955468	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs560294591	chr5:178955487-178955488	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs185017213	chr5:178955530-178955531	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs149535920	chr5:178955545-178955546	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs111671678	chr5:178955548-178955549	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs532829464	chr5:178955556-178955557	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs144081193	chr5:178955611-178955612	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs140464122	chr5:178955642-178955643	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs188539505	chr5:178955643-178955644	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs548615327	chr5:178955661-178955662	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs370589976	chr5:178955684-178955685	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2652 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178949400-178956600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr5:178951000-178957000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:178953200-178956600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr5:178953600-178954800	Enhancers	Hela-S3	cervix
5	chr5:178953600-178956400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr5:178953600-178956600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr5:178954200-178954600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr5:178954200-178954800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr5:178954400-178954600	Enhancers	Primary hematopoietic stem cells	blood
10	chr5:178954400-178954600	Enhancers	Spleen	Spleen
11	chr5:178954600-178954800	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr5:178954600-178954800	Enhancers	Thymus	Thymus
13	chr5:178954600-178956600	Weak transcription	Primary hematopoietic stem cells	blood
14	chr5:178954600-178956800	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr5:178954600-178957200	Weak transcription	Spleen	Spleen
16	chr5:178954800-178955000	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr5:178954800-178956600	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr5:178954800-178956600	Weak transcription	Thymus	Thymus
19	chr5:178954800-178957400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:178955000-178955200	Enhancers	Dnd41	blood
21	chr5:178955000-178956800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr5:178955200-178955400	Enhancers	Colon Smooth Muscle	Colon
23	chr5:178955200-178956600	Weak transcription	Dnd41	blood
24	chr5:178955400-178956600	Weak transcription	Colon Smooth Muscle	Colon
25	chr5:178955800-178956400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr5:178956400-178958800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr5:178956600-178956800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr5:178956600-178956800	Enhancers	Adipose Nuclei	Adipose
29	chr5:178956600-178956800	Enhancers	Duodenum Mucosa	Duodenum
30	chr5:178956600-178957000	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr5:178956600-178957000	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr5:178956600-178957000	Enhancers	Colon Smooth Muscle	Colon
33	chr5:178956600-178957000	Enhancers	Thymus	Thymus
34	chr5:178956600-178957400	Flanking Active TSS	Primary hematopoietic stem cells	blood
35	chr5:178956600-178957400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr5:178956600-178957800	Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr5:178956600-178958200	Active TSS	GM12878-XiMat	blood
38	chr5:178956600-178958800	Flanking Active TSS	Dnd41	blood
39	chr5:178956800-178957000	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr5:178956800-178957000	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr5:178956800-178957000	Enhancers	Primary B cells from peripheral blood	blood
42	chr5:178956800-178957000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr5:178956800-178957000	Enhancers	Fetal Thymus	thymus
44	chr5:178956800-178957000	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr5:178956800-178957200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr5:178956800-178957200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr5:178956800-178957200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
48	chr5:178956800-178957400	Flanking Active TSS	Duodenum Mucosa	Duodenum
49	chr5:178956800-178957800	Flanking Active TSS	Adipose Nuclei	Adipose
50	chr5:178956800-178957800	Active TSS	Duodenum Smooth Muscle	Duodenum

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